Regio‐, Diastereo‐, and Enantioselective Synthesis of vic‐Diols via α‐Silyl Ketones According to the SAMP/RAMP Hydrazone Method
- 25 January 1991
- journal article
- research article
- Published by Wiley in European Journal of Inorganic Chemistry
- Vol. 124 (1) , 219-226
- https://doi.org/10.1002/cber.19911240133
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- A formal total synthesis of erythromycin A. 1. Facile and stereoselective syntheses of erythronolide a segments based on acyclic stereocontrolTetrahedron Letters, 1988
- Oxidative cleavage reactions of the silicon-carbon bonds. A new methodology for polyol synthesis.Journal of Synthetic Organic Chemistry, Japan, 1988
- (S)-(−)-1-AMINO-2-METHOXYMETHYLPYRROLIDINE (SAMP) AND (R)-(+)-1-AMINO-2-METHOXYMETHYLPYRROLIDINE (RAMP), VERSATILE CHIRAL AUXILIARIESOrganic Syntheses, 1987
- Prostaglandin synthesis. 12. Synthesis of (7E)- and (7Z)-punaglandin 4. Structural revisionJournal of the American Chemical Society, 1986
- Synthesis of lipoxin bTetrahedron Letters, 1986
- Stereocontrolled total synthesis of lipoxins AJournal of the American Chemical Society, 1985
- Alkylation of Chiral HydrazonesPublished by Elsevier ,1984
- Acyclic Stereoselective Synthesis of CarbohydratesJournal of Carbohydrate Chemistry, 1984
- Total Synthesis of the L-HexosesScience, 1983
- The infrared spectra of monoalkoxy(methyl)chlorosilanes and mono(chloroalkoxy)methylchlorosilanesCollection of Czechoslovak Chemical Communications, 1977